Evidence map›Paper›PMID 36500481›Full record

ArticleMolecules (Basel, Switzerland)2022

New MgFeAl-LDH Catalysts for Claisen-Schmidt Condensation.

Rodica Zăvoianu, Mădălina Tudorache, Vasile I Parvulescu, Bogdan Cojocaru, Octavian D Pavel

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.5field-weighted citation impact, top 42% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 7 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Rodica ZăvoianuFaculty of Chemistry, University of Bucharest, 4-12 Regina Elisabeta Avenue, 030018 Bucharest, Romania.ORCID 0000-0003-1271-9955
Mădălina TudoracheFaculty of Chemistry, University of Bucharest, 4-12 Regina Elisabeta Avenue, 030018 Bucharest, Romania.ORCID 0000-0003-1380-5214
Vasile I ParvulescuFaculty of Chemistry, University of Bucharest, 4-12 Regina Elisabeta Avenue, 030018 Bucharest, Romania.
Bogdan CojocaruFaculty of Chemistry, University of Bucharest, 4-12 Regina Elisabeta Avenue, 030018 Bucharest, Romania.ORCID 0000-0002-2019-4370
Octavian D PavelFaculty of Chemistry, University of Bucharest, 4-12 Regina Elisabeta Avenue, 030018 Bucharest, Romania.ORCID 0000-0002-6466-651X
University of Bucharest · RO

Funding

Unitatea Executiva Pentru Finantarea Invatamantului Superior a Cercetarii Dezvoltarii si Inovarii PN-III-P2-2.1-PED-2021-1870Unitatea Executiva Pentru Finantarea Invatamantului Superior a Cercetarii Dezvoltarii si Inovarii PN-III-P4-ID-PCE-2020-2207University of Bucharest C1.2.PFE_CDI.2021-587/Contract no.41PFE/30.12.2021
6 · The paper itself

Abstract

A rapid, cheap and feasible new approach was used to synthesize the Mg0.375Fe0.375Al0.25-LDH in the presence of tetramethylammonium hydroxide (TMAH), as a nontraditional hydrolysis agent, applying both mechano-chemical (MC) and co-precipitation methods (CP). For comparison, these catalysts were also synthesized using traditional inorganic alkalis. The mechano-chemical method brings several advantages since the number of steps and the energy involved are smaller than in the co-precipitation method, while the use of organic alkalis eliminates the possibility of contaminating the final solid with alkaline cations. The memory effect was also investigated. XRD studies showed Fe3O4 as stable phase in all solids. Regardless of the alkalis and synthesis methods used, the basicity of catalysts followed the trend: mixed oxides > parent LDH > hydrated LDH. The catalytic activity of the catalysts in the Claisen−Schmidt condensation between benzaldehyde and cyclohexanone showed a linear dependence to the basicity values. After 2 h, the calcined sample cLDH-CO32−/OH−-CP provided a conversion value of 93% with a total selectivity toward 2,6-dibenzylidenecyclohexanone. The presence of these catalysts in the reaction media inhibited the oxidation of benzaldehyde to benzoic acid. Meanwhile, for the self-condensation of cyclohexanone, the conversions to mono- and di-condensed compounds did not exceed 3.8%.

Indexed as

OxidesCatalysisOxidation-ReductionOxidesClaisen–Schmidt condensationmechano-chemicalMgFeAl-LDHtetramethylammonium hydroxide

Identifiers

PMID36500481
PMCPMC9740334
OpenAlexW4311050684

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.